New Zealand Gazette – 1998 – No. 148

Page 3589

✨ Medicine Distribution Consents

17 SEPTEMBER NEW ZEALAND GAZETTE 3589

Schedule

Name and Strength	Form	Name and Address of Manufacturer	Proprietary Name (if any)
Ammonium chloride 25 mg/mL, diphenhydramine hydrochloride 2.5 mg/mL	Syrup	PSM Holdings Limited, Wiri, Auckland	Diphenacough
Bisacodyl 10 mg	Suppository	C B Fleet & Co Inc., Lynchburg, Virginia, United States of America	Fleet Laxative Suppositories
Metoclopramide hydrochloride 5 mg/mL	Injection, solution (syringe and polyamp)	Astra Pharmaceuticals Pty Limited, North Ryde, New South Wales, Australia	Metoclopramide
Ketoconazole 2% w/w	Shampoo	Douglas Pharmaceuticals Limited, Mount Wellington, Auckland	Sebizole
Basiliximab 20 mg Diluent: Water for injection	Injection, powder with diluent	Novartis Pharma AG., Basel, Switzerland Diluent: Novartis Pharma AG., Stein, Switzerland	Simulect
Cefaclor monohydrate 27.8 mg/mL, 55.6 mg/mL equivalent to 25 mg/mL, 50 mg/mL cefaclor anhydrous	Suspension, oral	Ranbaxy Laboratories Limited, Dewas, Madhya Pradesh, India	Locef
Cefaclor monohydrate 267.5 mg/mL, 535 mg equivalent to 250 mg, 500 mg cefaclor anhydrous	Capsules, powder filled	Ranbaxy Laboratories Limited, Dewas, Madhya Pradesh, India	Locef

Dated this 8th day of September 1998.

G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on the 20th day of February 1997.

g06558

Provisional Consent to the Distribution of a New Medicine

Pursuant to section 23 of the Medicines Act 1981, the Minister of Health hereby provisionally consents to the sale, supply or use in New Zealand of the new medicine set out in the Schedule hereto:

Schedule

Name and Strength	Form	Name and Address of Manufacturer	Proprietary Name (if any)
Lamivudine 5 mg/mL	Solution, oral	Glaxo Wellcome Operations, Speke, Liverpool, United Kingdom	Zeffix

Note: This consent is valid for 2 years from the date of publication of this notice.

Dated this 14th day of September 1998.

G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on the 20th day of February 1997.

g06685

Consent to the Distribution of a Changed Medicine

Pursuant to section 23 of the Medicines Act 1981, the Minister of Health hereby provisionally consents to the sale, supply or use in New Zealand of the changed medicine which was referred to the Minister of Health under the provisions of section 24 (5) of the Act and is set out in the Schedule hereto:

Schedule

Name and Strength	Form	Name and Address of Manufacturer	Proprietary Name (if any)
Lamivudine 100 mg	Tablet, film coated	Glaxo Wellcome Operations, Ware, Hertfordshire, United Kingdom	Zeffix

Note: This consent is valid for 2 years from the date of publication of this notice.

Dated this 14th day of September 1998.

G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on the 20th day of February 1997.

g06686

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VUW Te Waharoa — NZ Gazette 1998, No 148

NZLII — NZ Gazette 1998, No 148

Parliament House (depicted) was completed in 1918 and remains the primary seat of Parliament.

✨ LLM interpretation of page content

🏥 Consent to the Distribution of a New Medicine

Domain🏥 Health & Social Welfare
Dated8 September 1998
KeywordsMedicines Act 1981, New Medicine, Distribution
👩‍💼 Officials

G. R. Boyd, Chief Advisor, Regulation and Safety

🏥 Provisional Consent to the Distribution of a New Medicine

Domain🏥 Health & Social Welfare
Dated14 September 1998
KeywordsMedicines Act 1981, New Medicine, Provisional Consent, Distribution
👩‍💼 Officials

G. R. Boyd, Chief Advisor, Regulation and Safety

🏥 Consent to the Distribution of a Changed Medicine

Domain🏥 Health & Social Welfare
Dated14 September 1998
KeywordsMedicines Act 1981, Changed Medicine, Distribution
👩‍💼 Officials

G. R. Boyd, Chief Advisor, Regulation and Safety

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